Treatment pathway of bone sarcoma in children, adolescents, and young adults

When pediatric, adolescent, and young adult patients present with a bone sarcoma, treatment decisions, especially after relapse, are complex and require a multidisciplinary approach. This review presents scenarios commonly encountered in the therapy of bone sarcomas with the goal of objectively pres...

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Veröffentlicht in:Cancer 2017-06, Vol.123 (12), p.2206-2218
Hauptverfasser: Reed, Damon R., Hayashi, Masanori, Wagner, Lars, Binitie, Odion, Steppan, Diana A., Brohl, Andrew S., Shinohara, Eric T., Bridge, Julia A., Loeb, David M., Borinstein, Scott C., Isakoff, Michael S.
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Sprache:eng
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Zusammenfassung:When pediatric, adolescent, and young adult patients present with a bone sarcoma, treatment decisions, especially after relapse, are complex and require a multidisciplinary approach. This review presents scenarios commonly encountered in the therapy of bone sarcomas with the goal of objectively presenting a consensus, multidisciplinary management approach. Little variation was found in the authors' group with respect to local control or systemic therapy. Clinical trials were universally prioritized in all settings. Decisions regarding relapse therapies in the absence of a clinical trial had very minor variations initially, but a consensus was reached after a literature review and discussion. This review presents a concise document and figures as a starting point for evidence‐based care for patients with these rare diseases. This framework allows prospective decision making and prioritization of clinical trials. It is hoped that this framework will inspire and focus future clinical research and thus lead to new trials to improve efficacy and reduce toxicity. Cancer 2017;123:2206–2218. © 2017 American Cancer Society. This review presents a pathway for the management of common clinical scenarios that arise in the treatment of bone sarcomas in children, adolescents, and young adults. Clinical trials should be prioritized when they are available, and for those times when trials are unavailable, a consensus, multidisciplinary management approach to bone sarcomas is presented.
ISSN:0008-543X
1097-0142
DOI:10.1002/cncr.30589